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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849405Generated: October 26, 2026

Sodium Carbonate → 2-Methyl-3-nitro-6-phenylpyridine

https://huagongshe.com/reaction/849405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Chloro-6-methyl-3-nitropyridineHCID 1268230—
Reactant7-Bromo-2,3,4,5-tetrahydro-1-(1H-imidazol-4-ylmethyl)-4-(1-naphthalenylcarbonyl)-1H-1,4-benzodiazepine, hydrochlorideHCID 178479667—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-3-nitro-6-phenylpyridineHCID 14932963—

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of Compound B and 2-chloro-3-nitro-6-methylpyridine (0.42 g, 2.40 mmol) in THF (10 mL) was degassed with nitrogen. Tetrakistriphenylphosphine palladium (28 mg, 0.024 mmol) was added and the mixture was stirred 30 minutes. 25 Phenylboronic acid (0.44 g, 3.6 mmol) and 2M Na2CO3 (1.8 mL) were added and the mixture was heated at 75° C. for 17 hours and stirred at room temperature for 48 hours. Methylene chloride was added and the mixture was filtered through celite and partitioned. The mixture was washed with saturated aqueous NaHCO3, dried (magnesium sulfate), filtered and evaporated to afford 0.77 g of brown solid. Flash chromatography (silica, 10% ethyl acetate/hexanes) afforded 0.37 g of Compound C (72%) as an off white solid and 0.05 g of 2-phenyl-3-nitro-6-methylpyridine (10%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011029
Source datasetuspto-grants-2000_01
ORD IDord-a32d5c738da44ee385a620da10b56492
Source noteuspto-grants-2000_01